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Related Concept Videos

Experimental Determination of Chemical Formula02:37

Experimental Determination of Chemical Formula

The elemental makeup of a compound defines its chemical identity, and chemical formulas are the most concise way of representing this elemental makeup. When a compound’s formula is unknown, measuring the mass of its constituent elements is often the first step in determining the formula experimentally.
Cycloaddition Reactions: Overview01:16

Cycloaddition Reactions: Overview

Cycloadditions are one of the most valuable and effective synthesis routes to form cyclic compounds. These are concerted pericyclic reactions between two unsaturated compounds resulting in a cyclic product with two new σ bonds formed at the expense of π bonds. The [4 + 2] cycloaddition, known as the Diels–Alder reaction, is the most common. The other example is a [2 + 2] cycloaddition.
Limitations of Friedel–Crafts Reactions01:26

Limitations of Friedel–Crafts Reactions

Several restrictions limit the use of Friedel–Crafts reactions. First, the halogen in the alkyl halide must be attached to an sp3-hybridized carbon for the Friedel–Crafts reactions to occur. Vinyl or aryl halides do not react since the carbocations formed are unstable under the reaction conditions. Second, Friedel–Crafts alkylation is susceptible to carbocation rearrangement, and the major products obtained have a rearranged carbon skeleton. In contrast, the acylium ion is stabilized by...
Inductive Effects on Chemical Shift: Overview01:27

Inductive Effects on Chemical Shift: Overview

The protons in unsubstituted alkanes are strongly shielded with chemical shifts below 1.8 ppm. Methine, methylene, and methyl protons appear at approximately 1.7, 1.2 and 0.7 ppm, while the proton signal from methane appears at 0.23 ppm. An electronegative substituent, such as chlorine, withdraws the electron density from the protons, increasing their chemical shift. Progressive substitution of the hydrogens in methane by chlorine shifts the proton signals increasingly downfield, to 3.05 ppm in...
Chemical Reactions01:19

Chemical Reactions

A chemical reaction is a process by which the bonds in the atoms of substances are rearranged to generate new substances. Matter cannot be created or destroyed in a chemical reaction—the same type and number of atoms that make up the reactants are still present in the products. Merely, the rearrangement of chemical bonds produces new compounds.
Chemical Reactions Rearrange Atoms into New Substances
A chemical reaction takes starting materials—the reactants—and changes them into different...
Chemical Reactions02:26

Chemical Reactions

A balanced chemical equation provides the information of chemical formulas of the reactants and products involved in the chemical change. A reaction’s stoichiometry helps predict how much of the reactant is needed to produce the desired amount of product, or in some cases, how much product will be formed from a specific amount of the reactant.
The relative amounts of reactants and products represented in a balanced chemical equation are often referred to as stoichiometric amounts. However, in...

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Related Experiment Video

Updated: May 14, 2026

Curation of Computational Chemical Libraries Demonstrated with Alpha-Amino Acids
08:21

Curation of Computational Chemical Libraries Demonstrated with Alpha-Amino Acids

Published on: April 13, 2022

Will combinatorial chemistry keep its promise?

John Carroll

    Biotechnology Healthcare
    |February 9, 2013
    PubMed
    Summary
    This summary is machine-generated.

    Despite criticism, combinatorial chemistry (combichem) is evolving. Biotechnology firms are shifting from large, diverse compound libraries to smaller, more focused ones.

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    Applying Cheminformatics to Develop a Structure Searchable Database of Analytical Methods
    05:34

    Applying Cheminformatics to Develop a Structure Searchable Database of Analytical Methods

    Published on: June 6, 2025

    Related Experiment Videos

    Last Updated: May 14, 2026

    Curation of Computational Chemical Libraries Demonstrated with Alpha-Amino Acids
    08:21

    Curation of Computational Chemical Libraries Demonstrated with Alpha-Amino Acids

    Published on: April 13, 2022

    Applying Cheminformatics to Develop a Structure Searchable Database of Analytical Methods
    05:34

    Applying Cheminformatics to Develop a Structure Searchable Database of Analytical Methods

    Published on: June 6, 2025

    Area of Science:

    • Biotechnology
    • Medicinal Chemistry
    • Drug Discovery

    Background:

    • Combinatorial chemistry (combichem) has faced scrutiny regarding its efficiency and applicability.
    • Traditional combichem often involves generating vast, diverse compound libraries.

    Purpose of the Study:

    • To explore the ongoing relevance and adaptation of combichem technologies in biotechnology.
    • To highlight the strategic shift towards more targeted library approaches.

    Main Methods:

    • Analysis of current trends in biotech drug discovery strategies.
    • Review of evolving combichem methodologies.

    Main Results:

    • Combinatorial chemistry is not being abandoned despite challenges.
    • Biotechnology companies are implementing new combichem strategies.
    • There is a move from diverse compound libraries to smaller, targeted libraries.

    Conclusions:

    • The field of combinatorial chemistry is adapting to overcome past limitations.
    • Targeted library design represents a strategic advancement in combichem for drug discovery.